Home Cart 0 Sign in  

[ CAS No. 5464-68-6 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 5464-68-6
Chemical Structure| 5464-68-6
Structure of 5464-68-6 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 5464-68-6 ]

Related Doc. of [ 5464-68-6 ]

Alternatived Products of [ 5464-68-6 ]

Product Details of [ 5464-68-6 ]

CAS No. :5464-68-6 MDL No. :MFCD00014805
Formula : C6H14NO4P Boiling Point : -
Linear Structure Formula :- InChI Key :QPVCUQOSWAXEOQ-UHFFFAOYSA-N
M.W : 195.15 Pubchem ID :225722
Synonyms :

Calculated chemistry of [ 5464-68-6 ]

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.83
Num. rotatable bonds : 6
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 44.7
TPSA : 88.43 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -8.09 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.0
Log Po/w (XLOGP3) : -0.85
Log Po/w (WLOGP) : 0.74
Log Po/w (MLOGP) : -0.58
Log Po/w (SILICOS-IT) : -0.62
Consensus Log Po/w : -0.06

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -0.12
Solubility : 149.0 mg/ml ; 0.761 mol/l
Class : Very soluble
Log S (Ali) : -0.53
Solubility : 58.1 mg/ml ; 0.298 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.96
Solubility : 21.3 mg/ml ; 0.109 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.44

Safety of [ 5464-68-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P305+P351+P338 UN#:N/A
Hazard Statements:H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 5464-68-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 5464-68-6 ]
  • Downstream synthetic route of [ 5464-68-6 ]

[ 5464-68-6 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 79-07-2 ]
  • [ 122-52-1 ]
  • [ 5464-68-6 ]
YieldReaction ConditionsOperation in experiment
33% for 3.5 h; Reflux 2-Chloroacetamide (5.01 g, 53.6 mmol) and triethyl phosphite (9.19 mL, 53.6 mmol) were heated at reflux in o-xylene (14 mL) for 3.5 h. The solvent was removed under reduced pressure to afford a dark brown tar-like residue. The residue was taken up in dichloromethane and filtered through a short column of silica. The filtrate was concentrated and the solid recrystallised from ethyl acetate/pentane to afford diethyl carbamoylmethylphosphonate (3.42 g, 33percent) as light brown crystals. ‘H NMR (200 MHz, DMSO-d6) ö 7.35 (br s, 1H); 7.02 (br s, 1H); 4.02 (dq, 4H, J=7.1 Hz, JpH=1.1 Hz); 2.80(d, 2H, JPH =21.4 Hz); 1.23 (t, 6H, J=7.0 Hz). ‘3C NMR (50 MHz, DMSO-d6) ö 166.0(d, 2Jcp5.1 Hz); 61.5 (d, 2J=6.0 Hz); 34.5 (d, ‘Jp131.6 Hz); 16.2 (d, 3J=6.0 Hz).3’P NMR (81 MHz, DMSO-d6) 23.8. ESIMS: m/z 218 [M+Na]. HRMS calcd forC6H,4N04P 195.0655, found 195.0653.
Reference: [1] Journal of Organic Chemistry, 2009, vol. 74, # 23, p. 9140 - 9151
[2] Patent: WO2015/39173, 2015, A1, . Location in patent: Page/Page column 12; 13
[3] Journal of Organic Chemistry, 1959, vol. 24, p. 434
[4] Journal of Organic Chemistry, 1958, vol. 23, p. 1883,1885
[5] Pesticide Science, 1994, vol. 40, # 1, p. 57 - 62
  • 2
  • [ 867-13-0 ]
  • [ 5464-68-6 ]
Reference: [1] Chemische Berichte, 1924, vol. 57, p. 1030[2] Chemische Berichte, 1926, vol. 59, p. 1120
[3] Roczniki Chemii, 1963, vol. 37, p. 949 - 954
  • 3
  • [ 683-57-8 ]
  • [ 122-52-1 ]
  • [ 5464-68-6 ]
Reference: [1] Phosphorus, Sulfur and Silicon and Related Elements, 2000, vol. 160, p. 195 - 205
  • 4
  • [ 867-13-0 ]
  • [ 5464-68-6 ]
Reference: [1] Chemische Berichte, 1924, vol. 57, p. 1030[2] Chemische Berichte, 1926, vol. 59, p. 1120
Same Skeleton Products
Historical Records